Clinical and Model-Based Evaluation of the Effect of Glasdegib on Cardiac Repolarization From a Randomized Thorough QT Study

Clin Pharmacol Drug Dev. 2021 Mar;10(3):272-282. doi: 10.1002/cpdd.862. Epub 2020 Aug 12.

Abstract

Glasdegib is a potent, selective oral inhibitor of the Hedgehog signaling pathway. This phase 1 double-blind thorough QT study (NCT03162900) evaluated the effects of glasdegib on QTc interval. The study enrolled 36 healthy volunteers to receive a single dose of 150 mg glasdegib (representing a therapeutic dose), 300 mg glasdegib (representing a supratherapeutic dose), 400 mg moxifloxacin (positive control), or placebo under fasted conditions. The study demonstrated that therapeutic and supratherapeutic doses of glasdegib had no significant effect on QTc interval; the upper bound of the 2-sided 90% confidence intervals (CIs) for all time-matched least-squares mean differences in QT interval corrected using Fridericia's formula (QTcF) between glasdegib and placebo was below the prespecified criterion of 20 milliseconds (Food and Drug Administration correspondence reviewed and accepted). Based on an exposure-response analysis, glasdegib was determined not to have a meaningful effect on heart rate (change in RR interval). The mean (90%CI) model-derived baseline and placebo-adjusted QTcF at the average maximum observed concentration values corresponding to therapeutic and supratherapeutic glasdegib doses was 7.3 milliseconds (6.5-8.2 milliseconds) and 13.7 milliseconds (12.0-15.5 milliseconds), respectively. Together these results demonstrated that following therapeutic and supratherapeutic glasdegib dosing, the change in QTc from baseline was well below the 20-millisecond threshold of clinical concern in oncology.

Keywords: QTc; cardiac repolarization; exposure-response; glasdegib; safety.

Publication types

  • Clinical Trial, Phase I
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Benzimidazoles / pharmacokinetics*
  • Benzimidazoles / pharmacology
  • Case-Control Studies
  • Cross-Over Studies
  • Dose-Response Relationship, Drug
  • Double-Blind Method
  • Electrocardiography / drug effects
  • Electrocardiography / methods
  • Fasting
  • Healthy Volunteers / statistics & numerical data
  • Heart / drug effects*
  • Heart / physiology
  • Hedgehog Proteins / antagonists & inhibitors*
  • Humans
  • Male
  • Middle Aged
  • Moxifloxacin / administration & dosage
  • Phenylurea Compounds / pharmacokinetics*
  • Phenylurea Compounds / pharmacology
  • Placebos / administration & dosage
  • Smoothened Receptor / antagonists & inhibitors*
  • Topoisomerase II Inhibitors / administration & dosage

Substances

  • Benzimidazoles
  • Hedgehog Proteins
  • Phenylurea Compounds
  • Placebos
  • Smoothened Receptor
  • Topoisomerase II Inhibitors
  • glasdegib
  • Moxifloxacin

Associated data

  • ClinicalTrials.gov/NCT03162900